Welcome to the next event from the Health Talks series – health, life sciences and entrepreneurship talks organized by Aalto University, Health Design, Kuopio Health, OuluHealth, Terkko Health Hub, Upgraded – Health Startup Association of Finland, Health Hub Tampere, HealthTurku, HiLIFE and Healthtech Finland.
Health Talks is an events series focusing on health, life sciences and entrepreneurship. It covers a variety of contemporary as well as future topics relevant to innovative health and life science entrepreneurship. During the next webinar, this time co-hosted by OuluHealth, you will hear an insider’s view on medical device market entry and find out more about an MDR Fast Track service launched by Innokas Medical. The service enables medtech companies to outsource the regulatory burden, focus on their core, and reach profitable and growing business faster than via the traditional route.
Join the webinar to learn how to navigate the industry’s complex regulatory environment in new ways and ask your questions to get a deeper understanding of the service. Innokas Medical’s expert, Pekka Pohjosaho, will tell you what the MDR Fast Track means in real life, how to evaluate whether the service is a match for you and what steps to take to get started.
Time: 26 January 2023, 10:00 – 11:00
Place: Online
This event is free of charge, and it will be held in English.
Register for the event 👇
https://www.eventbrite.com/e/mdr-fast-track-service-how-to-enable-medical-device-market-entry-tickets-465313203317
Agenda
10:00 – 10:05 Opening words
10:05 -10:50 MDR Fast Track Service – How to enable medical device market entry with reasonable effort, Pekka Pohjosaho / Innokas Medical
10:50 – 11:00 Q & A
11:00 Closing words
The speaker
Head of Quality and Regulatory at Innokas Medical, Pekka Pohjosaho, is an experienced Quality and Regulatory professional with a long history of working in the medical device domain. Pekka has deep practical knowledge of applying the various requirements in the field, such as ISO 13485, ISO 14971, IEC 61010-1, IEC 62366, IEC 62304, MDSAP and MDR as well as hands-on experience in working with R&D projects of AIMD, MD and IVD products as QA/RA specialist, project manager, usability engineer and software quality engineer. Currently, leading the Innokas QARA team Pekka has a front-seat view of the development and challenges of today’s Medical Device industry.
How to join
The webinar will be held via Zoom. You will receive the link after registration.
Notes
Registration data is controlled by Terkko and shared with other Health Talks partners.
The event will be recorded and later shared with the public.
For more info check the Health Talks webpage: https://terkko.fi/health-talks/
We are excited to see you online very soon!